Description
Lithium 2-methylbutan-2-olate (CAS No. 53535-81-2) is a highly specialized organolithium compound with the molecular formula C5H11LiO. This reagent is widely utilized in synthetic organic chemistry, particularly in nucleophilic addition reactions and as a strong base for deprotonation processes. Its sterically hindered alkoxide structure enhances selectivity in reactions involving sensitive substrates. Packaged under inert conditions to ensure stability, this product is ideal for researchers and scientists requiring precise and reactive organometallic reagents. Suitable for use in anhydrous environments, it is commonly employed in pharmaceutical, agrochemical, and advanced material synthesis applications.
Properties
- CAS Number: 53535-81-2
- Complexity: 43.3
- IUPAC Name: lithium;2-methylbutan-2-olate
- InChI: InChI=1S/C5H11O.Li/c1-4-5(2,3)6;/h4H2,1-3H3;/q-1;+1
- InChI Key: QPDJILZPDAMLFH-UHFFFAOYSA-N
- Exact Mass: 94.09699340
- Molecular Formula: C5H11LiO
- Molecular Weight: 94.1
- SMILES: [Li+].CCC(C)(C)[O-]
- Topological: 23.1
- Monoisotopic Mass: 94.09699340
- Synonyms: Lithium 2-methylbutan-2-olate, 53535-81-2, lithium;2-methylbutan-2-olate, lithium t-pentoxide, SCHEMBL73825, DTXSID80635591, QPDJILZPDAMLFH-UHFFFAOYSA-N
Lithium 2-methylbutan-2-olate is primarily used as a strong, sterically hindered base in organic synthesis. It facilitates selective deprotonation of weakly acidic protons in ketones, esters, and other carbonyl compounds. Its applications extend to polymerization catalysts and as an intermediate in fine chemical production. Due to its reactivity, it is often handled under strict anhydrous and oxygen-free conditions.
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